Topical calcitriol enhances normal hair regrowth but does not prevent chemotherapy-induced alopecia in mice.

Using a murine model that mimics chemotherapy-induced alopecia (CIA) in humans particularly well, we show here that in contrast to previously reported CIA-protective effects in neonatal rats, topical calcitriol does not prevent CIA in adolescent mice but enhances the regrowth of normally pigmented hair shafts. When, prior to injecting 1 X 120 mg/kg cyclophosphamide i.p., 0.2 microg calcitriol or vehicle alone were administered topically to the back skin of C57BL/6 mice with all hair follicles in anagen, no significant macroscopic differences in the onset and severity of CIA were seen. However, hair shaft regrowth after CIA, which is often retarded and patchy, thus displaying severe and sometimes persistent pigmentation disorders, was significantly accelerated, enhanced, and qualitatively improved in test compared with control mice. Histomorphometric analysis suggests that this is related to the fact that calcitriol-pretreated follicles favor the "dystrophic catagen pathway" of response to chemical injury, ie., a follicular repair strategy allowing for the unusually fast reconstruction of a new, undamaged anagen hair bulb. Thus, it may be unrealistic to expect that topical calcitriol can prevent human CIA, but topical calcitriols may well enhance the regrowth of a normal hair coat.

[1]  J. Reichrath,et al.  Hair follicle expression of 1,25‐dihydroxyvitamin D3 receptors during the murine hair cycle , 1994, The British journal of dermatology.

[2]  S. Eichmüller,et al.  A murine model for inducing and manipulating hair follicle regression (catagen): effects of dexamethasone and cyclosporin A. , 1994, The Journal of investigative dermatology.

[3]  S. Eichmüller,et al.  Chemotherapy-induced alopecia in mice. Induction by cyclophosphamide, inhibition by cyclosporine A, and modulation by dexamethasone. , 1994, The American journal of pathology.

[4]  R. Paus,et al.  The "bulge-activation hypothesis" does not explain hair follicle cycling but may still be valid. , 1994, The American Journal of dermatopathology.

[5]  A. Chakraborty,et al.  Melanogenesis during the anagen-catagen-telogen transformation of the murine hair cycle. , 1993, The Journal of investigative dermatology.

[6]  R. Paus,et al.  Melanogenesis is coupled to murine anagen: toward new concepts for the role of melanocytes and the regulation of melanogenesis in hair growth. , 1993, The Journal of investigative dermatology.

[7]  J. Jimenez,et al.  Protection from chemotherapy-induced alopecia by 1,25-dihydroxyvitamin D3. , 1992, Cancer research.

[8]  J. Jimenez,et al.  Protection from 1-beta-D-arabinofuranosylcytosine-induced alopecia by epidermal growth factor and fibroblast growth factor in the rat model. , 1992, Cancer research.

[9]  J. Jimenez,et al.  Protection from chemotherapy-induced alopecia in a rat model. , 1990, Science.

[10]  R. Paus,et al.  Telogen skin contains an inhibitor of hair growth , 1990, The British journal of dermatology.

[11]  J E Coggle,et al.  The influence of the hair cycle on the thickness of mouse skin , 1984, The Anatomical record.

[12]  Thomas B. Fitzpatrick,et al.  Dermatology in general medicine , 1971 .

[13]  H. Wallace Diseases of the hair and scalp. , 1962, The Practitioner.